TY - JOUR
T1 - Adsorption of Chromate Ions by Layered Double Hydroxide–Bentonite Nanocomposite for Groundwater Remediation
AU - Kim, Yoogyeong
AU - Son, Yeongkyun
AU - Bae, Sungjun
AU - Kim, Tae Hyun
AU - Hwang, Yuhoon
N1 - Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2022/4/1
Y1 - 2022/4/1
N2 - Herein, magnesium/aluminum-layered double hydroxide (MgAl-LDH) and bentonite (BT) nanocomposites (LDH–BT) were prepared by co-precipitation (CP), exfoliation–reassembly (ER), and simple solid-phase hybridization (SP). The prepared LDH–BT nanocomposites were pre-liminarily characterized by using powder X-ray diffractometry, scanning electron microscopy, and zeta-potentiometry. The chromate adsorption efficacies of the pristine materials (LDH and benton-ite) and the as-prepared nanocomposites were investigated. Among the composites, the LDH– BT_SP was found to exhibit the highest chromate removal efficiency of 65.7%. The effect of varying the LDH amount in the LDH–BT composite was further investigated, and a positive relationship between the LDH ratio and chromate removal efficiency was identified. The chromate adsorption by the LDH–BT_SP was performed under various concentrations (isotherm) and contact times (ki-netic). The results of the isotherm experiments were well fitted with the Langmuir and Freundlich isotherm model and demonstrate multilayer chromate adsorption by the heterogeneous LDH– BT_SP, with a homogenous distribution of LDH nanoparticles. The mobility of the as-prepared LDH–BT_SP was investigated on a silica sand-filled column to demonstrate that the mobility of the bentonite is dramatically decreased after hybridization with LDH. Furthermore, when the LDH– BT_SP was injected into a box container filled with silica sand to simulate subsurface soil conditions, the chromate removal efficacy was around 43% in 170 min. Thus, it was confirmed that the LDH– BT prepared by solid-phase hybridization is a practical clay-based nanocomposite for in situ soil and groundwater remediation.
AB - Herein, magnesium/aluminum-layered double hydroxide (MgAl-LDH) and bentonite (BT) nanocomposites (LDH–BT) were prepared by co-precipitation (CP), exfoliation–reassembly (ER), and simple solid-phase hybridization (SP). The prepared LDH–BT nanocomposites were pre-liminarily characterized by using powder X-ray diffractometry, scanning electron microscopy, and zeta-potentiometry. The chromate adsorption efficacies of the pristine materials (LDH and benton-ite) and the as-prepared nanocomposites were investigated. Among the composites, the LDH– BT_SP was found to exhibit the highest chromate removal efficiency of 65.7%. The effect of varying the LDH amount in the LDH–BT composite was further investigated, and a positive relationship between the LDH ratio and chromate removal efficiency was identified. The chromate adsorption by the LDH–BT_SP was performed under various concentrations (isotherm) and contact times (ki-netic). The results of the isotherm experiments were well fitted with the Langmuir and Freundlich isotherm model and demonstrate multilayer chromate adsorption by the heterogeneous LDH– BT_SP, with a homogenous distribution of LDH nanoparticles. The mobility of the as-prepared LDH–BT_SP was investigated on a silica sand-filled column to demonstrate that the mobility of the bentonite is dramatically decreased after hybridization with LDH. Furthermore, when the LDH– BT_SP was injected into a box container filled with silica sand to simulate subsurface soil conditions, the chromate removal efficacy was around 43% in 170 min. Thus, it was confirmed that the LDH– BT prepared by solid-phase hybridization is a practical clay-based nanocomposite for in situ soil and groundwater remediation.
KW - bentonite
KW - chromate adsorption
KW - groundwater remediation
KW - layered double hydroxide
KW - nanocomposite
UR - http://www.scopus.com/inward/record.url?scp=85128476019&partnerID=8YFLogxK
U2 - 10.3390/nano12081384
DO - 10.3390/nano12081384
M3 - Article
AN - SCOPUS:85128476019
SN - 2079-4991
VL - 12
JO - Nanomaterials
JF - Nanomaterials
IS - 8
M1 - 1384
ER -